ENST00000399503.4:c.2766C>T
MANE Select
|
ENSP00000382423.3:p.Ala922=
|
|
ENST00000399503.3:c.2766C>T
|
ENSP00000382423.3:p.Ala922=
|
|
NM_005921.1:c.2766C>T
|
NP_005912.1:p.Ala922=
|
|
XM_005248519.3:c.2388C>T
|
XP_005248576.2:p.Ala796=
|
|
XM_011543406.1:c.2511C>T
|
XP_011541708.1:p.Ala837=
|
|
XM_011543407.1:c.2487C>T
|
XP_011541709.1:p.Ala829=
|
|
XM_011543408.1:c.2766C>T
|
XP_011541710.1:p.Ala922=
|
|
XM_017009484.1:c.2355C>T
|
XP_016864973.1:p.Ala785=
|
|
XM_017009485.1:c.2277C>T
|
XP_016864974.1:p.Ala759=
|
|
XR_001742068.2:n.2797C>T
|
|
|
NM_005921.2:c.2766C>T
MANE Select
|
NP_005912.1:p.Ala922=
|
|